Moser Michael A J, Sawicka Katherine, Arcand Steven, O'Brien Preston, Luke Patrick, Beck Gavin, Sawicka Jolanta, Cohen Alejandro, Sawicki Grzegorz
Department of Surgery, University of Saskatchewan, Saskatoon, Canada.
Department of Pharmacology, University of Saskatchewan, Saskatoon, Canada.
Ann Transplant. 2017 Dec 8;22:730-739. doi: 10.12659/aot.905347.
BACKGROUND Machine cold perfusion is beneficial to the preservation of kidneys for transplantation. At the end of preservation, the perfusion solution contains many proteins. Using a proteomics approach, we searched for useful biomarkers and potential therapeutic targets in the perfusate. Our program is unique in that all transplant kidneys (even living donor kidneys, LKD) are placed on machine cold perfusion prior to transplantation. MATERIAL AND METHODS Perfusates from donation after neurological and circulatory determination of death (DNDD and DCDD respectively) and LKD were collected (n=41) and analyzed for LDH, neutrophil gelatinase-associated lipocalin (NGAL), and matrix metalloproteinase-2 (MMP-2) as markers of injury. Perfusate from each kidney was subjected to 2-dimensional gel electrophoresis, then analyzed using software to identify those spots which are significantly different between the 3 groups. Mass spectrometry was used to identify the proteins and their identity was confirmed with Western blot. RESULTS The highest levels of MMP-2, LDH, and NGAL were seen for the DCDD kidneys, followed by the DNDD kidneys and then LDK. Peroxiredoxin-2, NGAL, and alpha-1-antitrypsin were identified as significantly different between the different types of donor kidneys, and their role and possible therapeutic strategies are discussed. Collagen fragments, albumin, and immunoglobulin were also identified as possible byproducts of the injury and may be useful is assessing the degree of injury. CONCLUSIONS Comparison of the perfusates from the different types of kidneys has allowed us to identify proteins that will be useful in future research into reducing injury in transplant kidneys.
背景 机器冷灌注有利于肾脏移植保存。保存结束时,灌注液中含有许多蛋白质。我们采用蛋白质组学方法,在灌注液中寻找有用的生物标志物和潜在治疗靶点。我们的方案独特之处在于,所有移植肾(甚至活体供肾,LKD)在移植前均进行机器冷灌注。
材料与方法 收集来自神经学判定死亡后捐献(DNDD)和循环判定死亡后捐献(DCDD)以及活体供肾的灌注液(n = 41),并分析其中的乳酸脱氢酶(LDH)、中性粒细胞明胶酶相关脂质运载蛋白(NGAL)和基质金属蛋白酶-2(MMP-2)作为损伤标志物。对每个肾脏的灌注液进行二维凝胶电泳,然后使用软件分析以识别三组之间有显著差异的斑点。采用质谱法鉴定蛋白质,并通过蛋白质印迹法确认其身份。
结果 DCDD肾脏的MMP-2、LDH和NGAL水平最高,其次是DNDD肾脏,然后是LKD。过氧化物酶体增殖物激活受体-2、NGAL和α-1抗胰蛋白酶在不同类型供体肾脏之间存在显著差异,并对其作用和可能的治疗策略进行了讨论。胶原片段、白蛋白和免疫球蛋白也被鉴定为可能的损伤副产物,可能有助于评估损伤程度。
结论 对不同类型肾脏的灌注液进行比较,使我们能够识别出对未来减少移植肾损伤研究有用的蛋白质。